Estimating the Cost of Spinopelvic Complications After Adult Spinal Deformity Surgery.

deformity surgery sacroiliac spinopelvic

Journal

ClinicoEconomics and outcomes research : CEOR
ISSN: 1178-6981
Titre abrégé: Clinicoecon Outcomes Res
Pays: New Zealand
ID NLM: 101560564

Informations de publication

Date de publication:
2023
Historique:
received: 20 09 2023
accepted: 01 11 2023
medline: 15 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: epublish

Résumé

Reoperations for spinopelvic failure after adult spinal deformity (ASD) surgery are common. We sought to determine the added costs of ASD surgery attributable to reoperations for spinopelvic construct failures. We constructed a Markov process model to calculate the expected discounted 5-year costs of spinopelvic construct failures after ASD surgery. The Nationwide Inpatient Sample (NIS) was queried to estimate the number of ASD surgeries. Model inputs were based on literature review and expert opinion. ASD surgery was defined as thoracolumbar fusion of 4 or more levels with pelvic fixation. The following pelvic fixation failures were included: 1) rod fracture or pseudarthrosis from L4-S1, 2) iliac screw failure or set plug dislodgment, 3) iliac screw prominence, and 4) sacroiliac (SI) joint pain. The number of patients undergoing ASD surgery annually in the US was determined using a commercial claims database. The net present value 5-year cost per patient for spinopelvic complications was $35,265, equal to 29% of index surgery costs. Given an estimated 27,580 cases annually in the US, the additional cost to address spinopelvic complications reach nearly $1 billion over 5-years. A sensitivity analysis showed that these costs were most sensitive to the rate of rod fracture/pseudarthrosis, iliac screw prominence, and reoperation. A conservative estimate of the cost of spinopelvic failures after ASD surgery is substantial, nearly $1 billion over 5-years. We propose a method of capturing spinopelvic fixation failures for use in future clinical studies and cost analyses.

Identifiants

pubmed: 37964981
doi: 10.2147/CEOR.S437202
pii: 437202
pmc: PMC10642569
doi:

Types de publication

Journal Article

Langues

eng

Pagination

765-772

Informations de copyright

© 2023 Zuckerman et al.

Déclaration de conflit d'intérêts

Dr Daniel Cher and Dr Robyn Capobianco are employees of SI-BONE. SI-BONE manufactures devices used in spine surgery. The manuscript does not discuss these devices. Dr Daniel Sciubba reports personal fees from DePuy, Medtronic, Stryker, Nuvasive, Baxter, and SI Bone, outside the submitted work. Dr David Polly reports personal fees from SI Bone and Globus, during the conduct of the study; grants from Medtronic and MizuhoOSI, outside the submitted work. In addition, Dr David Polly has patents US 11,571,245 B2. February 7, 2023, US 11,234,830 B2. February 1, 2022, and US 11,369,419 B2. June 28, 2022 with royalties paid to SI Bone. The authors report no other conflicts of interest in this work.

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Auteurs

Scott L Zuckerman (SL)

Department of Neurological Surgery, Vanderbilt University Medical Center, Nashville, TN, USA.

Daniel Cher (D)

SI-BONE, Inc, Santa Clara, CA, USA.

Robyn Capobianco (R)

SI-BONE, Inc, Santa Clara, CA, USA.

Daniel Sciubba (D)

Department of Neurosurgery, Zucker School of Medicine at Hofstra, Long Island Jewish Medical Center and North Shore University Hospital, Northwell Health, Manhasset, NY, USA.

David W Polly (DW)

Department of Orthopaedic Surgery, University of Minnesota, Minneapolis, MN, USA.

Classifications MeSH